Synergistic effect of transition metal oxides and ozone on PCDD/F destruction

Catalytic oxidations of PCDD/Fs (polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans) with ozone on the transition metal oxides (iron oxide or manganese oxide) at the temperature range of 120–180 °C were investigated. These two catalysts were prepared by precipitation methods. Iron o...

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Veröffentlicht in:Journal of hazardous materials 2009-05, Vol.164 (2), p.1452-1459
Hauptverfasser: Wang, Hou Chuan, Chang, Shu Hao, Hung, Pao Chang, Hwang, Jyh Feng, Chang, Moo Been
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Sprache:eng
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Zusammenfassung:Catalytic oxidations of PCDD/Fs (polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans) with ozone on the transition metal oxides (iron oxide or manganese oxide) at the temperature range of 120–180 °C were investigated. These two catalysts were prepared by precipitation methods. Iron oxide has a higher surface area (330 m 2/g) than manganese oxide (53 m 2/g). In the absence of ozone, the removal efficiencies of PCDD/Fs achieved with iron oxide or manganese oxide were between 83% and 85%, while the destruction efficiencies were only between 20% and 25% at 180 °C. It indicates that adsorption was the main removal mechanism of PCDD/Fs over these two catalysts. On the other hand, ozone addition greatly enhanced the catalytic activity of iron oxide or manganese oxide catalysts on the oxidation of gaseous PCDD/Fs. At 180 °C, the destruction efficiencies of gaseous PCDD/Fs achieved with iron oxide or manganese oxide with 100 ppm O 3 exceeded 90%. It indicates that catalytic ozonation achieved with iron oxide or manganese oxide is effective in decomposing PCDD/Fs and the application of ozone lowers the reaction temperature of PCDD/F oxidation below 200 °C. Furthermore, the synergistic effect of iron oxide and ozone is superior to that of manganese oxide due to the fact that the surface of iron oxide has more hydroxyl groups, which easily form hydrogen bonds with ozone and decompose to form atomic oxygen for the further reaction with dioxin molecules.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2008.09.093